Clinical Research Associate, U.S. Expert Network

This is a fully remote position, open to applicants in New York.

📋 Description

• Become a part of Alcedis’s U.S.-based network of seasoned Clinical Research Associates.

• Assist with ongoing and upcoming clinical studies within the Clinical Operations team as new projects emerge.

• Execute and facilitate Site Initiation Visits, predominantly in a virtual setting, across the U.S. and Canada.

• Carry out on-site and remote monitoring activities for clinical trials.

• Collaborate with clinical research experts and peers across both U.S. and European time zones.

• Engage in part-time project work for the duration of mutually agreed assignments.

• Discuss the scope, timing, workload, and availability when a suitable project arises.

⛳️ Requirements

• Over 3 years of practical experience as a Clinical Research Associate (CRA) or Clinical Monitor.

• Experience in GCP-regulated interventional clinical trials.

• Proven experience in oncology clinical trials.

• Direct experience with digital clinical trial solutions, including ePRO, eCOA, and eCRF systems.

• Capability to work independently and proactively with a strong sense of ownership.

• Experience in both on-site and remote monitoring activities.

• Willingness to conduct and support Site Initiation Visits primarily in a virtual format across the U.S. and Canada.

• Strong communication and organizational skills.

• Excellent proficiency in written and spoken English.

• Must be located in the United States.

• Preferred: experience in Neurology and/or Alzheimer’s disease.

• Preferred: background working in international or cross-border clinical research teams.

• Preferred: ability and flexibility to collaborate across U.S. and European time zones, including regular communication with colleagues based in Germany.

• Preferred: familiarity with U.S. and Canadian clinical trial regulations.

• Preferred: knowledge of FDA regulations, HIPAA, and 21 CFR Part 11.

🏝️ Benefits

• Part-time W-2 employment on a project basis for the duration of a specific project.

• Flexible participation aligned with project requirements and mutual availability.

• Opportunity to continue working with other clients outside of the agreed assignment, adhering to confidentiality and conflict-of-interest policies.

• Compensation for necessary project-specific qualification or pre-engagement activities that require actual work beyond the application and selection process.

• Access to select clinical trial projects through the expert network.